CA3015744C - Utilisation de 1-[2-[[1-(4-chlorophenyle)pyrazol-3-yl]oxymethyle]-3-methyle-phenyle]-4-methyle-tetrazol-5-one pour lutter contre les champignonsphytopathogenes resistants sur les cereales - Google Patents
Utilisation de 1-[2-[[1-(4-chlorophenyle)pyrazol-3-yl]oxymethyle]-3-methyle-phenyle]-4-methyle-tetrazol-5-one pour lutter contre les champignonsphytopathogenes resistants sur les cereales Download PDFInfo
- Publication number
- CA3015744C CA3015744C CA3015744A CA3015744A CA3015744C CA 3015744 C CA3015744 C CA 3015744C CA 3015744 A CA3015744 A CA 3015744A CA 3015744 A CA3015744 A CA 3015744A CA 3015744 C CA3015744 C CA 3015744C
- Authority
- CA
- Canada
- Prior art keywords
- compound
- methyl
- trifluoromethyl
- fungi
- cereals
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Active
Links
- 241000233866 Fungi Species 0.000 title claims abstract description 151
- 235000013339 cereals Nutrition 0.000 title claims abstract description 130
- 230000003032 phytopathogenic effect Effects 0.000 title claims abstract description 22
- XUQQRGKFXLAPNV-UHFFFAOYSA-N metyltetraprole Chemical compound CC1=CC=CC(N2C(N(C)N=N2)=O)=C1COC(=N1)C=CN1C1=CC=C(Cl)C=C1 XUQQRGKFXLAPNV-UHFFFAOYSA-N 0.000 title abstract description 4
- 150000001875 compounds Chemical class 0.000 claims abstract description 103
- 239000003112 inhibitor Substances 0.000 claims abstract description 25
- 230000035772 mutation Effects 0.000 claims abstract description 17
- 239000000463 material Substances 0.000 claims abstract description 11
- 238000000034 method Methods 0.000 claims abstract description 9
- 108010075028 Cytochromes b Proteins 0.000 claims abstract description 8
- 230000002438 mitochondrial effect Effects 0.000 claims abstract description 7
- 238000009395 breeding Methods 0.000 claims abstract description 5
- 230000001488 breeding effect Effects 0.000 claims abstract description 5
- 230000002538 fungal effect Effects 0.000 claims abstract description 4
- 239000002689 soil Substances 0.000 claims abstract description 4
- 239000000203 mixture Substances 0.000 claims description 109
- 241000209140 Triticum Species 0.000 claims description 47
- 235000021307 Triticum Nutrition 0.000 claims description 47
- 241000209219 Hordeum Species 0.000 claims description 45
- 235000007340 Hordeum vulgare Nutrition 0.000 claims description 45
- 239000005788 Fluxapyroxad Substances 0.000 claims description 27
- 239000005810 Metrafenone Substances 0.000 claims description 27
- HTSGKJQDMSTCGS-UHFFFAOYSA-N 1,4-bis(4-chlorophenyl)-2-(4-methylphenyl)sulfonylbutane-1,4-dione Chemical compound C1=CC(C)=CC=C1S(=O)(=O)C(C(=O)C=1C=CC(Cl)=CC=1)CC(=O)C1=CC=C(Cl)C=C1 HTSGKJQDMSTCGS-UHFFFAOYSA-N 0.000 claims description 26
- 241000196324 Embryophyta Species 0.000 claims description 26
- 239000005730 Azoxystrobin Substances 0.000 claims description 24
- 241001360088 Zymoseptoria tritici Species 0.000 claims description 24
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 23
- SXSGXWCSHSVPGB-UHFFFAOYSA-N fluxapyroxad Chemical compound FC(F)C1=NN(C)C=C1C(=O)NC1=CC=CC=C1C1=CC(F)=C(F)C(F)=C1 SXSGXWCSHSVPGB-UHFFFAOYSA-N 0.000 claims description 21
- AMSPWOYQQAWRRM-UHFFFAOYSA-N metrafenone Chemical compound COC1=CC=C(Br)C(C)=C1C(=O)C1=C(C)C=C(OC)C(OC)=C1OC AMSPWOYQQAWRRM-UHFFFAOYSA-N 0.000 claims description 21
- 241000520648 Pyrenophora teres Species 0.000 claims description 20
- WFDXOXNFNRHQEC-GHRIWEEISA-N azoxystrobin Chemical compound CO\C=C(\C(=O)OC)C1=CC=CC=C1OC1=CC(OC=2C(=CC=CC=2)C#N)=NC=N1 WFDXOXNFNRHQEC-GHRIWEEISA-N 0.000 claims description 19
- -1 metconzole Chemical compound 0.000 claims description 17
- 239000005869 Pyraclostrobin Substances 0.000 claims description 15
- 241000173769 Ramularia collo-cygni Species 0.000 claims description 14
- 239000005738 Bixafen Substances 0.000 claims description 12
- HZRSNVGNWUDEFX-UHFFFAOYSA-N pyraclostrobin Chemical compound COC(=O)N(OC)C1=CC=CC=C1COC1=NN(C=2C=CC(Cl)=CC=2)C=C1 HZRSNVGNWUDEFX-UHFFFAOYSA-N 0.000 claims description 12
- 239000005737 Benzovindiflupyr Substances 0.000 claims description 11
- 239000005758 Cyprodinil Substances 0.000 claims description 11
- MNHVNIJQQRJYDH-UHFFFAOYSA-N 2-[2-(1-chlorocyclopropyl)-3-(2-chlorophenyl)-2-hydroxypropyl]-1,2-dihydro-1,2,4-triazole-3-thione Chemical compound N1=CNC(=S)N1CC(C1(Cl)CC1)(O)CC1=CC=CC=C1Cl MNHVNIJQQRJYDH-UHFFFAOYSA-N 0.000 claims description 10
- 239000005825 Prothioconazole Substances 0.000 claims description 10
- 125000004289 pyrazol-3-yl group Chemical group [H]N1N=C(*)C([H])=C1[H] 0.000 claims description 10
- DGOAXBPOVUPPEB-UHFFFAOYSA-N 3-(difluoromethyl)-N-methoxy-1-methyl-N-[1-(2,4,6-trichlorophenyl)propan-2-yl]pyrazole-4-carboxamide Chemical compound C=1N(C)N=C(C(F)F)C=1C(=O)N(OC)C(C)CC1=C(Cl)C=C(Cl)C=C1Cl DGOAXBPOVUPPEB-UHFFFAOYSA-N 0.000 claims description 9
- 239000005741 Bromuconazole Substances 0.000 claims description 9
- 239000005747 Chlorothalonil Substances 0.000 claims description 9
- 239000005760 Difenoconazole Substances 0.000 claims description 9
- 239000005822 Propiconazole Substances 0.000 claims description 9
- LDLMOOXUCMHBMZ-UHFFFAOYSA-N bixafen Chemical compound FC(F)C1=NN(C)C=C1C(=O)NC1=CC=C(F)C=C1C1=CC=C(Cl)C(Cl)=C1 LDLMOOXUCMHBMZ-UHFFFAOYSA-N 0.000 claims description 9
- HJJVPARKXDDIQD-UHFFFAOYSA-N bromuconazole Chemical compound ClC1=CC(Cl)=CC=C1C1(CN2N=CN=C2)OCC(Br)C1 HJJVPARKXDDIQD-UHFFFAOYSA-N 0.000 claims description 9
- CRQQGFGUEAVUIL-UHFFFAOYSA-N chlorothalonil Chemical compound ClC1=C(Cl)C(C#N)=C(Cl)C(C#N)=C1Cl CRQQGFGUEAVUIL-UHFFFAOYSA-N 0.000 claims description 9
- HAORKNGNJCEJBX-UHFFFAOYSA-N cyprodinil Chemical compound N=1C(C)=CC(C2CC2)=NC=1NC1=CC=CC=C1 HAORKNGNJCEJBX-UHFFFAOYSA-N 0.000 claims description 9
- BQYJATMQXGBDHF-UHFFFAOYSA-N difenoconazole Chemical compound O1C(C)COC1(C=1C(=CC(OC=2C=CC(Cl)=CC=2)=CC=1)Cl)CN1N=CN=C1 BQYJATMQXGBDHF-UHFFFAOYSA-N 0.000 claims description 9
- STJLVHWMYQXCPB-UHFFFAOYSA-N propiconazole Chemical compound O1C(CCC)COC1(C=1C(=CC(Cl)=CC=1)Cl)CN1N=CN=C1 STJLVHWMYQXCPB-UHFFFAOYSA-N 0.000 claims description 9
- 241000895502 Blumeria graminis f. sp. tritici Species 0.000 claims description 8
- CCCGEKHKTPTUHJ-UHFFFAOYSA-N N-[9-(dichloromethylene)-1,2,3,4-tetrahydro-1,4-methanonaphthalen-5-yl]-3-(difluoromethyl)-1-methylpyrazole-4-carboxamide Chemical compound FC(F)C1=NN(C)C=C1C(=O)NC1=CC=CC2=C1C1CCC2C1=C(Cl)Cl CCCGEKHKTPTUHJ-UHFFFAOYSA-N 0.000 claims description 8
- 241000190117 Pyrenophora tritici-repentis Species 0.000 claims description 8
- 241001515790 Rhynchosporium secalis Species 0.000 claims description 8
- ZMYFCFLJBGAQRS-IRXDYDNUSA-N (2R,3S)-epoxiconazole Chemical compound C1=CC(F)=CC=C1[C@@]1(CN2N=CN=C2)[C@H](C=2C(=CC=CC=2)Cl)O1 ZMYFCFLJBGAQRS-IRXDYDNUSA-N 0.000 claims description 6
- RYAUSSKQMZRMAI-ALOPSCKCSA-N (2S,6R)-4-[3-(4-tert-butylphenyl)-2-methylpropyl]-2,6-dimethylmorpholine Chemical compound C=1C=C(C(C)(C)C)C=CC=1CC(C)CN1C[C@H](C)O[C@H](C)C1 RYAUSSKQMZRMAI-ALOPSCKCSA-N 0.000 claims description 6
- MGNFYQILYYYUBS-UHFFFAOYSA-N 1-[3-(4-tert-butylphenyl)-2-methylpropyl]piperidine Chemical compound C=1C=C(C(C)(C)C)C=CC=1CC(C)CN1CCCCC1 MGNFYQILYYYUBS-UHFFFAOYSA-N 0.000 claims description 6
- PFFIDZXUXFLSSR-UHFFFAOYSA-N 1-methyl-N-[2-(4-methylpentan-2-yl)-3-thienyl]-3-(trifluoromethyl)pyrazole-4-carboxamide Chemical compound S1C=CC(NC(=O)C=2C(=NN(C)C=2)C(F)(F)F)=C1C(C)CC(C)C PFFIDZXUXFLSSR-UHFFFAOYSA-N 0.000 claims description 6
- PDPWCKVFIFAQIQ-UHFFFAOYSA-N 2-{2-[(2,5-dimethylphenoxy)methyl]phenyl}-2-methoxy-N-methylacetamide Chemical compound CNC(=O)C(OC)C1=CC=CC=C1COC1=CC(C)=CC=C1C PDPWCKVFIFAQIQ-UHFFFAOYSA-N 0.000 claims description 6
- 239000005740 Boscalid Substances 0.000 claims description 6
- 239000005767 Epoxiconazole Substances 0.000 claims description 6
- 239000005777 Fenpropidin Substances 0.000 claims description 6
- 239000005778 Fenpropimorph Substances 0.000 claims description 6
- 239000005783 Fluopyram Substances 0.000 claims description 6
- 239000005789 Folpet Substances 0.000 claims description 6
- 239000005799 Isopyrazam Substances 0.000 claims description 6
- 239000005803 Mandestrobin Substances 0.000 claims description 6
- 239000005816 Penthiopyrad Substances 0.000 claims description 6
- 239000005818 Picoxystrobin Substances 0.000 claims description 6
- 239000005837 Spiroxamine Substances 0.000 claims description 6
- 239000005857 Trifloxystrobin Substances 0.000 claims description 6
- WYEMLYFITZORAB-UHFFFAOYSA-N boscalid Chemical compound C1=CC(Cl)=CC=C1C1=CC=CC=C1NC(=O)C1=CC=CN=C1Cl WYEMLYFITZORAB-UHFFFAOYSA-N 0.000 claims description 6
- 229940118790 boscalid Drugs 0.000 claims description 6
- KVDJTXBXMWJJEF-UHFFFAOYSA-N fluopyram Chemical compound ClC1=CC(C(F)(F)F)=CN=C1CCNC(=O)C1=CC=CC=C1C(F)(F)F KVDJTXBXMWJJEF-UHFFFAOYSA-N 0.000 claims description 6
- HKIOYBQGHSTUDB-UHFFFAOYSA-N folpet Chemical compound C1=CC=C2C(=O)N(SC(Cl)(Cl)Cl)C(=O)C2=C1 HKIOYBQGHSTUDB-UHFFFAOYSA-N 0.000 claims description 6
- HIIRDDUVRXCDBN-OBGWFSINSA-N metominostrobin Chemical compound CNC(=O)C(=N\OC)\C1=CC=CC=C1OC1=CC=CC=C1 HIIRDDUVRXCDBN-OBGWFSINSA-N 0.000 claims description 6
- PUYXTUJWRLOUCW-UHFFFAOYSA-N spiroxamine Chemical compound O1C(CN(CC)CCC)COC11CCC(C(C)(C)C)CC1 PUYXTUJWRLOUCW-UHFFFAOYSA-N 0.000 claims description 6
- ONCZDRURRATYFI-TVJDWZFNSA-N trifloxystrobin Chemical compound CO\N=C(\C(=O)OC)C1=CC=CC=C1CO\N=C(/C)C1=CC=CC(C(F)(F)F)=C1 ONCZDRURRATYFI-TVJDWZFNSA-N 0.000 claims description 6
- LRCCWFKSGWHDQR-UHFFFAOYSA-N 1-methyl-3-(trifluoromethyl)-n-(1,1,3-trimethyl-2,3-dihydroinden-4-yl)pyrazole-4-carboxamide Chemical compound C=12C(C)CC(C)(C)C2=CC=CC=1NC(=O)C1=CN(C)N=C1C(F)(F)F LRCCWFKSGWHDQR-UHFFFAOYSA-N 0.000 claims description 5
- KNUJXXAPWWVVAG-UHFFFAOYSA-N 3-(difluoromethyl)-1,5-dimethyl-n-(1,1,3-trimethyl-2,3-dihydroinden-4-yl)pyrazole-4-carboxamide Chemical compound C=12C(C)CC(C)(C)C2=CC=CC=1NC(=O)C1=C(C)N(C)N=C1C(F)F KNUJXXAPWWVVAG-UHFFFAOYSA-N 0.000 claims description 5
- YTCIYOXHHQLDEI-UHFFFAOYSA-N 3-(difluoromethyl)-1-methyl-n-(1,1,3-trimethyl-2,3-dihydroinden-4-yl)pyrazole-4-carboxamide Chemical compound C=12C(C)CC(C)(C)C2=CC=CC=1NC(=O)C1=CN(C)N=C1C(F)F YTCIYOXHHQLDEI-UHFFFAOYSA-N 0.000 claims description 5
- XTDZGXBTXBEZDN-UHFFFAOYSA-N 3-(difluoromethyl)-N-(9-isopropyl-1,2,3,4-tetrahydro-1,4-methanonaphthalen-5-yl)-1-methylpyrazole-4-carboxamide Chemical compound CC(C)C1C2CCC1C1=C2C=CC=C1NC(=O)C1=CN(C)N=C1C(F)F XTDZGXBTXBEZDN-UHFFFAOYSA-N 0.000 claims description 5
- IBSNKSODLGJUMQ-SDNWHVSQSA-N picoxystrobin Chemical compound CO\C=C(\C(=O)OC)C1=CC=CC=C1COC1=CC=CC(C(F)(F)F)=N1 IBSNKSODLGJUMQ-SDNWHVSQSA-N 0.000 claims description 5
- MEUXXHGDZUDAAW-UHFFFAOYSA-N 1,3,5-trimethyl-n-(1,1,3-trimethyl-2,3-dihydroinden-4-yl)pyrazole-4-carboxamide Chemical compound C=12C(C)CC(C)(C)C2=CC=CC=1NC(=O)C=1C(C)=NN(C)C=1C MEUXXHGDZUDAAW-UHFFFAOYSA-N 0.000 claims description 4
- SBYGUIUIDOUGBU-UHFFFAOYSA-N 1,5-dimethyl-3-(trifluoromethyl)-n-(1,1,3-trimethyl-2,3-dihydroinden-4-yl)pyrazole-4-carboxamide Chemical compound C=12C(C)CC(C)(C)C2=CC=CC=1NC(=O)C1=C(C)N(C)N=C1C(F)(F)F SBYGUIUIDOUGBU-UHFFFAOYSA-N 0.000 claims description 4
- 241000895523 Blumeria graminis f. sp. hordei Species 0.000 claims description 2
- 241001515786 Rhynchosporium Species 0.000 claims description 2
- RFFVPMBIBPQADE-UHFFFAOYSA-N 2,5-dimethyl-N-(1,1,3-trimethyl-2,3-dihydroinden-4-yl)-1H-pyrazole-5-carboxamide Chemical compound CN1NC(C=C1)(C(=O)NC1=C2C(CC(C2=CC=C1)(C)C)C)C RFFVPMBIBPQADE-UHFFFAOYSA-N 0.000 claims 1
- JERZEQUMJNCPRJ-UHFFFAOYSA-N 2-[4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl]-1-(1H-1,2,4-triazol-1-yl)propan-2-ol Chemical compound C=1C=C(OC=2C=CC(Cl)=CC=2)C=C(C(F)(F)F)C=1C(O)(C)CN1C=NC=N1 JERZEQUMJNCPRJ-UHFFFAOYSA-N 0.000 claims 1
- SIIJJFOXEOHODQ-UHFFFAOYSA-N 2-[4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl]-3-methyl-1-(1,2,4-triazol-1-yl)butan-2-ol Chemical compound C=1C=C(OC=2C=CC(Cl)=CC=2)C=C(C(F)(F)F)C=1C(O)(C(C)C)CN1C=NC=N1 SIIJJFOXEOHODQ-UHFFFAOYSA-N 0.000 claims 1
- QGTOTYJSCYHYFK-FWKSHIOASA-N CC(C(=O)OCOC=1C(=NC=CC1OC)C(NC1C(O[C@H]([C@@H]([C@H](C(OC1)=O)CC1=CC=CC=C1)OC(C(C)C)=O)C)=O)=O)C Chemical compound CC(C(=O)OCOC=1C(=NC=CC1OC)C(NC1C(O[C@H]([C@@H]([C@H](C(OC1)=O)CC1=CC=CC=C1)OC(C(C)C)=O)C)=O)=O)C QGTOTYJSCYHYFK-FWKSHIOASA-N 0.000 claims 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 28
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 24
- BTANRVKWQNVYAZ-UHFFFAOYSA-N Sec-butyl alcohol Natural products CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 description 16
- YXXPNGIZHZHBTQ-UHFFFAOYSA-N butan-2-ol Chemical compound CC[C](C)O YXXPNGIZHZHBTQ-UHFFFAOYSA-N 0.000 description 16
- 235000014113 dietary fatty acids Nutrition 0.000 description 15
- 239000000194 fatty acid Substances 0.000 description 15
- 229930195729 fatty acid Natural products 0.000 description 15
- 239000013543 active substance Substances 0.000 description 13
- 239000004094 surface-active agent Substances 0.000 description 11
- 239000000839 emulsion Substances 0.000 description 10
- 150000004665 fatty acids Chemical class 0.000 description 10
- 150000003871 sulfonates Chemical class 0.000 description 10
- 239000000725 suspension Substances 0.000 description 10
- 239000012895 dilution Substances 0.000 description 9
- 238000010790 dilution Methods 0.000 description 9
- KQNPFQTWMSNSAP-UHFFFAOYSA-N isobutyric acid Chemical compound CC(C)C(O)=O KQNPFQTWMSNSAP-UHFFFAOYSA-N 0.000 description 9
- 230000000694 effects Effects 0.000 description 8
- 239000003960 organic solvent Substances 0.000 description 8
- 244000052769 pathogen Species 0.000 description 8
- 239000000843 powder Substances 0.000 description 8
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 7
- 239000002270 dispersing agent Substances 0.000 description 7
- 239000000243 solution Substances 0.000 description 7
- 241001480061 Blumeria graminis Species 0.000 description 6
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
- 150000001298 alcohols Chemical class 0.000 description 6
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 6
- 239000003086 colorant Substances 0.000 description 6
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 6
- 239000004495 emulsifiable concentrate Substances 0.000 description 6
- 235000019198 oils Nutrition 0.000 description 6
- 239000007921 spray Substances 0.000 description 6
- 239000002671 adjuvant Substances 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 5
- 239000003995 emulsifying agent Substances 0.000 description 5
- 239000008187 granular material Substances 0.000 description 5
- 239000007787 solid Substances 0.000 description 5
- 239000011550 stock solution Substances 0.000 description 5
- QYPFLRIVEVOAGA-UHFFFAOYSA-N 1,3-dimethyl-n-(1,1,3-trimethyl-2,3-dihydroinden-4-yl)pyrazole-4-carboxamide Chemical compound C=12C(C)CC(C)(C)C2=CC=CC=1NC(=O)C1=CN(C)N=C1C QYPFLRIVEVOAGA-UHFFFAOYSA-N 0.000 description 4
- LWQPNBSCXAHNRY-UHFFFAOYSA-N 3-[4-(aminomethyl)-6-(trifluoromethyl)pyridin-2-yl]oxy-N-(2-hydroxyethyl)-N-methylbenzamide Chemical compound NCC1=CC(=NC(=C1)C(F)(F)F)OC=1C=C(C(=O)N(C)CCO)C=CC=1 LWQPNBSCXAHNRY-UHFFFAOYSA-N 0.000 description 4
- 241000221785 Erysiphales Species 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 239000000969 carrier Substances 0.000 description 4
- 239000000084 colloidal system Substances 0.000 description 4
- 229940125904 compound 1 Drugs 0.000 description 4
- 239000004491 dispersible concentrate Substances 0.000 description 4
- 239000006185 dispersion Substances 0.000 description 4
- 239000000417 fungicide Substances 0.000 description 4
- 239000000499 gel Substances 0.000 description 4
- 235000012054 meals Nutrition 0.000 description 4
- 239000004530 micro-emulsion Substances 0.000 description 4
- 239000003921 oil Substances 0.000 description 4
- 230000003647 oxidation Effects 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- 229920002451 polyvinyl alcohol Polymers 0.000 description 4
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 4
- 230000001681 protective effect Effects 0.000 description 4
- 229920005552 sodium lignosulfonate Polymers 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 239000002562 thickening agent Substances 0.000 description 4
- 239000000080 wetting agent Substances 0.000 description 4
- XAGZJIQIVXSURR-UHFFFAOYSA-N 1-[4-(trifluoromethyl)phenyl]piperidin-2-one Chemical group C1=CC(C(F)(F)F)=CC=C1N1C(=O)CCCC1 XAGZJIQIVXSURR-UHFFFAOYSA-N 0.000 description 3
- 108010052832 Cytochromes Proteins 0.000 description 3
- 102000018832 Cytochromes Human genes 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- 101710122864 Major tegument protein Proteins 0.000 description 3
- 101710148592 PTS system fructose-like EIIA component Proteins 0.000 description 3
- 101710169713 PTS system fructose-specific EIIA component Proteins 0.000 description 3
- 239000004372 Polyvinyl alcohol Substances 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 229930182692 Strobilurin Natural products 0.000 description 3
- 101710199973 Tail tube protein Proteins 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 241000607479 Yersinia pestis Species 0.000 description 3
- 238000010521 absorption reaction Methods 0.000 description 3
- 239000008186 active pharmaceutical agent Substances 0.000 description 3
- 150000001412 amines Chemical class 0.000 description 3
- 230000000844 anti-bacterial effect Effects 0.000 description 3
- 239000002518 antifoaming agent Substances 0.000 description 3
- 239000003899 bactericide agent Substances 0.000 description 3
- 239000011230 binding agent Substances 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 238000010410 dusting Methods 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 238000007710 freezing Methods 0.000 description 3
- 238000011081 inoculation Methods 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 239000003094 microcapsule Substances 0.000 description 3
- 239000000178 monomer Substances 0.000 description 3
- 150000002790 naphthalenes Chemical class 0.000 description 3
- 229920006395 saturated elastomer Polymers 0.000 description 3
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 3
- 125000004201 2,4-dichlorophenyl group Chemical group [H]C1=C([H])C(*)=C(Cl)C([H])=C1Cl 0.000 description 2
- YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 description 2
- VGAVFMUCIIYQFJ-UHFFFAOYSA-N CON=C(C(=O)NC)C(=CC)C Chemical compound CON=C(C(=O)NC)C(=CC)C VGAVFMUCIIYQFJ-UHFFFAOYSA-N 0.000 description 2
- 102000015782 Electron Transport Complex III Human genes 0.000 description 2
- 108010024882 Electron Transport Complex III Proteins 0.000 description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- 229910019142 PO4 Inorganic materials 0.000 description 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
- 239000003905 agrochemical Substances 0.000 description 2
- 239000012872 agrochemical composition Substances 0.000 description 2
- 235000012211 aluminium silicate Nutrition 0.000 description 2
- 150000001408 amides Chemical class 0.000 description 2
- 239000002280 amphoteric surfactant Substances 0.000 description 2
- 239000003945 anionic surfactant Substances 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 2
- 239000002775 capsule Substances 0.000 description 2
- 235000013877 carbamide Nutrition 0.000 description 2
- 150000007942 carboxylates Chemical class 0.000 description 2
- 239000004359 castor oil Substances 0.000 description 2
- 235000019438 castor oil Nutrition 0.000 description 2
- 239000003093 cationic surfactant Substances 0.000 description 2
- 201000010099 disease Diseases 0.000 description 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- 239000010685 fatty oil Substances 0.000 description 2
- 239000003337 fertilizer Substances 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 244000053095 fungal pathogen Species 0.000 description 2
- 230000000855 fungicidal effect Effects 0.000 description 2
- 150000004676 glycans Chemical class 0.000 description 2
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 2
- 239000004009 herbicide Substances 0.000 description 2
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 230000002401 inhibitory effect Effects 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 239000002917 insecticide Substances 0.000 description 2
- 239000012528 membrane Substances 0.000 description 2
- 235000010755 mineral Nutrition 0.000 description 2
- 239000002480 mineral oil Substances 0.000 description 2
- 210000003470 mitochondria Anatomy 0.000 description 2
- 239000002736 nonionic surfactant Substances 0.000 description 2
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 2
- 239000006072 paste Substances 0.000 description 2
- 230000001717 pathogenic effect Effects 0.000 description 2
- 230000000361 pesticidal effect Effects 0.000 description 2
- 239000000575 pesticide Substances 0.000 description 2
- 235000021317 phosphate Nutrition 0.000 description 2
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 2
- 229920000867 polyelectrolyte Polymers 0.000 description 2
- 229920001451 polypropylene glycol Polymers 0.000 description 2
- 229920001282 polysaccharide Polymers 0.000 description 2
- 239000005017 polysaccharide Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 238000003825 pressing Methods 0.000 description 2
- 230000029058 respiratory gaseous exchange Effects 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 150000004760 silicates Chemical class 0.000 description 2
- 238000006467 substitution reaction Methods 0.000 description 2
- 235000013311 vegetables Nutrition 0.000 description 2
- 239000000230 xanthan gum Substances 0.000 description 2
- 229920001285 xanthan gum Polymers 0.000 description 2
- 235000010493 xanthan gum Nutrition 0.000 description 2
- 229940082509 xanthan gum Drugs 0.000 description 2
- QFLWZFQWSBQYPS-AWRAUJHKSA-N (3S)-3-[[(2S)-2-[[(2S)-2-[5-[(3aS,6aR)-2-oxo-1,3,3a,4,6,6a-hexahydrothieno[3,4-d]imidazol-4-yl]pentanoylamino]-3-methylbutanoyl]amino]-3-(4-hydroxyphenyl)propanoyl]amino]-4-[1-bis(4-chlorophenoxy)phosphorylbutylamino]-4-oxobutanoic acid Chemical compound CCCC(NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)CCCCC1SC[C@@H]2NC(=O)N[C@H]12)C(C)C)P(=O)(Oc1ccc(Cl)cc1)Oc1ccc(Cl)cc1 QFLWZFQWSBQYPS-AWRAUJHKSA-N 0.000 description 1
- KANAPVJGZDNSCZ-UHFFFAOYSA-N 1,2-benzothiazole 1-oxide Chemical class C1=CC=C2S(=O)N=CC2=C1 KANAPVJGZDNSCZ-UHFFFAOYSA-N 0.000 description 1
- VUWCWMOCWKCZTA-UHFFFAOYSA-N 1,2-thiazol-4-one Chemical class O=C1CSN=C1 VUWCWMOCWKCZTA-UHFFFAOYSA-N 0.000 description 1
- HWGJWYNMDPTGTD-UHFFFAOYSA-N 1h-azonine Chemical compound C=1C=CC=CNC=CC=1 HWGJWYNMDPTGTD-UHFFFAOYSA-N 0.000 description 1
- ZVXKYWHJBYIYNI-UHFFFAOYSA-N 1h-pyrazole-4-carboxamide Chemical compound NC(=O)C=1C=NNC=1 ZVXKYWHJBYIYNI-UHFFFAOYSA-N 0.000 description 1
- PAWQVTBBRAZDMG-UHFFFAOYSA-N 2-(3-bromo-2-fluorophenyl)acetic acid Chemical compound OC(=O)CC1=CC=CC(Br)=C1F PAWQVTBBRAZDMG-UHFFFAOYSA-N 0.000 description 1
- CKDDMXSSWVFPGO-UHFFFAOYSA-N 2-methylpent-3-enamide Chemical compound CC=CC(C)C(N)=O CKDDMXSSWVFPGO-UHFFFAOYSA-N 0.000 description 1
- BCFOOQRXUXKJCL-UHFFFAOYSA-N 4-amino-4-oxo-2-sulfobutanoic acid Chemical class NC(=O)CC(C(O)=O)S(O)(=O)=O BCFOOQRXUXKJCL-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 239000004254 Ammonium phosphate Substances 0.000 description 1
- LVDKZNITIUWNER-UHFFFAOYSA-N Bronopol Chemical compound OCC(Br)(CO)[N+]([O-])=O LVDKZNITIUWNER-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical class OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- 235000019738 Limestone Nutrition 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical class OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 1
- 229920002873 Polyethylenimine Polymers 0.000 description 1
- 229920002396 Polyurea Polymers 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 229930006000 Sucrose Natural products 0.000 description 1
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical class OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- VJHCJDRQFCCTHL-UHFFFAOYSA-N acetic acid 2,3,4,5,6-pentahydroxyhexanal Chemical compound CC(O)=O.OCC(O)C(O)C(O)C(O)C=O VJHCJDRQFCCTHL-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 150000001447 alkali salts Chemical class 0.000 description 1
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
- 125000005599 alkyl carboxylate group Chemical group 0.000 description 1
- 125000000539 amino acid group Chemical group 0.000 description 1
- 229910000148 ammonium phosphate Inorganic materials 0.000 description 1
- 235000019289 ammonium phosphates Nutrition 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 1
- 235000011130 ammonium sulphate Nutrition 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000005667 attractant Substances 0.000 description 1
- OGBUMNBNEWYMNJ-UHFFFAOYSA-N batilol Chemical class CCCCCCCCCCCCCCCCCCOCC(O)CO OGBUMNBNEWYMNJ-UHFFFAOYSA-N 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 229960003168 bronopol Drugs 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- OOCMUZJPDXYRFD-UHFFFAOYSA-L calcium;2-dodecylbenzenesulfonate Chemical compound [Ca+2].CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O.CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O OOCMUZJPDXYRFD-UHFFFAOYSA-L 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 150000003857 carboxamides Chemical class 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 238000012656 cationic ring opening polymerization Methods 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 229920003086 cellulose ether Polymers 0.000 description 1
- 125000000068 chlorophenyl group Chemical group 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 description 1
- 125000004188 dichlorophenyl group Chemical group 0.000 description 1
- 239000002283 diesel fuel Substances 0.000 description 1
- QKIUAMUSENSFQQ-UHFFFAOYSA-N dimethylazanide Chemical compound C[N-]C QKIUAMUSENSFQQ-UHFFFAOYSA-N 0.000 description 1
- 230000003467 diminishing effect Effects 0.000 description 1
- YRIUSKIDOIARQF-UHFFFAOYSA-N dodecyl benzenesulfonate Chemical compound CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 YRIUSKIDOIARQF-UHFFFAOYSA-N 0.000 description 1
- 229940071161 dodecylbenzenesulfonate Drugs 0.000 description 1
- 239000010459 dolomite Substances 0.000 description 1
- 229910000514 dolomite Inorganic materials 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 125000005610 enamide group Chemical group 0.000 description 1
- 239000003623 enhancer Substances 0.000 description 1
- WDAXFOBOLVPGLV-UHFFFAOYSA-N ethyl isobutyrate Chemical compound CCOC(=O)C(C)C WDAXFOBOLVPGLV-UHFFFAOYSA-N 0.000 description 1
- 230000009969 flowable effect Effects 0.000 description 1
- 108010023700 galanin-(1-13)-bradykinin-(2-9)-amide Proteins 0.000 description 1
- 230000035784 germination Effects 0.000 description 1
- 150000002303 glucose derivatives Chemical class 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 150000002314 glycerols Chemical class 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 238000005469 granulation Methods 0.000 description 1
- 230000003179 granulation Effects 0.000 description 1
- 239000003630 growth substance Substances 0.000 description 1
- 239000003906 humectant Substances 0.000 description 1
- 125000001165 hydrophobic group Chemical group 0.000 description 1
- 150000002462 imidazolines Chemical class 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 230000000749 insecticidal effect Effects 0.000 description 1
- VRWKTAYJTKRVCU-UHFFFAOYSA-N iron(6+);hexacyanide Chemical compound [Fe+6].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-] VRWKTAYJTKRVCU-UHFFFAOYSA-N 0.000 description 1
- 238000003973 irrigation Methods 0.000 description 1
- 230000002262 irrigation Effects 0.000 description 1
- KQNPFQTWMSNSAP-UHFFFAOYSA-M isobutyrate Chemical compound CC(C)C([O-])=O KQNPFQTWMSNSAP-UHFFFAOYSA-M 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 150000003893 lactate salts Chemical class 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 239000006028 limestone Substances 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- 239000011785 micronutrient Substances 0.000 description 1
- 235000013369 micronutrients Nutrition 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- XCZZVEYJQVLRPB-UHFFFAOYSA-N n,3-dimethylpent-3-enamide Chemical compound CNC(=O)CC(C)=CC XCZZVEYJQVLRPB-UHFFFAOYSA-N 0.000 description 1
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 235000010603 pastilles Nutrition 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 239000003961 penetration enhancing agent Substances 0.000 description 1
- 239000004477 pesticide formulation type Substances 0.000 description 1
- WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 1
- 231100000208 phytotoxic Toxicity 0.000 description 1
- 230000000885 phytotoxic effect Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 229920005646 polycarboxylate Polymers 0.000 description 1
- 229920000193 polymethacrylate Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 235000013772 propylene glycol Nutrition 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 150000003856 quaternary ammonium compounds Chemical class 0.000 description 1
- 238000010526 radical polymerization reaction Methods 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 239000005871 repellent Substances 0.000 description 1
- 230000002940 repellent Effects 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 239000004550 soluble concentrate Substances 0.000 description 1
- 238000009331 sowing Methods 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 238000001694 spray drying Methods 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000000021 stimulant Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 208000024891 symptom Diseases 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 235000012222 talc Nutrition 0.000 description 1
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 1
- MCVUKOYZUCWLQQ-UHFFFAOYSA-N tridecylbenzene Chemical class CCCCCCCCCCCCCC1=CC=CC=C1 MCVUKOYZUCWLQQ-UHFFFAOYSA-N 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 229940117958 vinyl acetate Drugs 0.000 description 1
- 239000004562 water dispersible granule Substances 0.000 description 1
- 239000003021 water soluble solvent Substances 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/713—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with four or more nitrogen atoms as the only ring hetero atoms
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/647—Triazoles; Hydrogenated triazoles
- A01N43/653—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
La présente invention concerne l'utilisation de tétrazolinones facultativement en combinaison avec d'autres pesticides pour combattre des champignons phytopathogènes résistants sur des céréales.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP16160599.3 | 2016-03-16 | ||
EP16160599 | 2016-03-16 | ||
PCT/EP2017/055946 WO2017157910A1 (fr) | 2016-03-16 | 2017-03-14 | Utilisation de tétrazolinones pour lutter contre des champignons phytopathogènes résistants sur des céréales |
Publications (2)
Publication Number | Publication Date |
---|---|
CA3015744A1 CA3015744A1 (fr) | 2017-09-21 |
CA3015744C true CA3015744C (fr) | 2024-04-23 |
Family
ID=55542489
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA3015744A Active CA3015744C (fr) | 2016-03-16 | 2017-03-14 | Utilisation de 1-[2-[[1-(4-chlorophenyle)pyrazol-3-yl]oxymethyle]-3-methyle-phenyle]-4-methyle-tetrazol-5-one pour lutter contre les champignonsphytopathogenes resistants sur les cereales |
Country Status (7)
Country | Link |
---|---|
US (1) | US10905122B2 (fr) |
EP (1) | EP3429357A1 (fr) |
JP (1) | JP6903074B2 (fr) |
CA (1) | CA3015744C (fr) |
RU (1) | RU2754614C2 (fr) |
UA (1) | UA125210C2 (fr) |
WO (1) | WO2017157910A1 (fr) |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
UA120628C2 (uk) | 2014-11-07 | 2020-01-10 | Басф Се | Пестицидні суміші |
US11241012B2 (en) | 2016-03-16 | 2022-02-08 | Basf Se | Use of tetrazolinones for combating resistant phytopathogenic fungi on soybean |
EP3429358A1 (fr) | 2016-03-16 | 2019-01-23 | Basf Se | Utilisation de tétrazolinones pour lutter contre des champignons phytopathogènes résistants sur des fruits |
BR122022025239B1 (pt) | 2016-10-10 | 2023-10-31 | Basf Se | Mistura pesticida, composição pesticida, métodos para controlar pragas fitopatogênicas, para melhorar a saúde de plantas e para a proteção do material de propagação vegetal contra pragas e material de propagação vegetal |
EP3648604A1 (fr) | 2017-07-05 | 2020-05-13 | BASF Agro B.V. | Mélanges fongicides de méfentrifluconazole |
EP3533333A1 (fr) * | 2018-03-02 | 2019-09-04 | Basf Se | Mélanges fongicides comprenant du pydiflumetofène |
JP2022518129A (ja) | 2018-12-31 | 2022-03-14 | アダマ・マクテシム・リミテッド | 殺真菌混合物 |
FR3096872A1 (fr) * | 2019-06-05 | 2020-12-11 | UPL Corporation Limited | composition fongicide pour lutter contre l'infection zymoseptoria chez la plante |
BR112022004977A2 (pt) * | 2019-09-19 | 2022-06-21 | Syngenta Crop Protection Ag | Método para controlar fungo |
Family Cites Families (202)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2526660A (en) | 1946-07-06 | 1950-10-24 | Rohm & Haas | Capryldintrophenyl crotonate |
DE2325878A1 (de) | 1973-05-22 | 1974-12-12 | Kalk Chemische Fabrik Gmbh | Phenoxyderivate des trifluormethylbenzols und verfahren zu deren herstellung |
GB1543964A (en) | 1976-04-08 | 1979-04-11 | Ici Ltd | Method of antagonising herbicides on soyabean and cotton |
DE2656747C2 (de) | 1976-12-15 | 1984-07-05 | Basf Ag, 6700 Ludwigshafen | Morpholinderivate |
DE2725314A1 (de) | 1977-06-04 | 1978-12-14 | Bayer Ag | 1-(2-phenylaethyl)-triazolium-salze, verfahren zu ihrer herstellung sowie ihre verwendung als fungizide |
CH647513A5 (de) | 1979-11-13 | 1985-01-31 | Sandoz Ag | Triazol-derivate, deren herstellung und verwendung. |
JPS5764632A (en) | 1980-10-09 | 1982-04-19 | Mitsui Toatsu Chem Inc | Novel 2-arylethyl ether derivative and thioether derivative, their production and insecticide and acaricide |
DE3140276A1 (de) | 1981-10-10 | 1983-04-28 | Bayer Ag, 5090 Leverkusen | Phenoxyphenyl-azolylmethyl-ketone und -carbinole, verfahren zu ihrer herstellung und ihre verwendung als fungizide und als zwischenprodukte |
PH19709A (en) | 1982-11-23 | 1986-06-16 | Ciba Geigy Ag | Microbicidal 1-carbonyl-1-phenoxyphenyl-2-azolylethanol derivatives |
BG48681A3 (en) | 1982-12-14 | 1991-04-15 | Ciba Geigy Ag | Fungicide means |
DE3484968D1 (de) | 1983-05-19 | 1991-10-02 | Ciba Geigy Ag | Verfahren zur herstellung von 1-triazolylethylether-derivaten, sowie mikrobizide mittel enthaltende neue 1-triazolyl-phenoxyphenylethylether-derivate als wirkstoffe und deren verwendung. |
EP0275955B1 (fr) | 1987-01-21 | 1990-07-04 | Ciba-Geigy Ag | Composition microbicide |
DE3801233A1 (de) | 1987-01-21 | 1988-08-04 | Ciba Geigy Ag | Mikrobizides mittel |
DE3733755A1 (de) | 1987-10-06 | 1989-04-20 | Bayer Ag | Verfahren zur herstellung von 2-(4-chlorphenyl-ethyl)-2-tert.-butyl-oxiran |
DE58903329D1 (de) | 1988-08-04 | 1993-03-04 | Ciba Geigy Ag | Mikrobizide mittel. |
DE58903327D1 (de) | 1988-08-04 | 1993-03-04 | Ciba Geigy Ag | Mikrobizide mittel. |
US4940720A (en) | 1989-08-02 | 1990-07-10 | Ciba-Geigy Corporation | Microbicidal compositions |
DE4003180A1 (de) | 1990-02-03 | 1991-08-08 | Bayer Ag | Halogenallyl-azolyl-derivate |
DE4025204A1 (de) | 1990-08-09 | 1992-02-13 | Bayer Ag | Halogenalkyl-azolyl-derivate |
EP0470466A3 (en) | 1990-08-09 | 1992-07-29 | Bayer Ag | Halogenalkyl-azolyl derivatives |
GB9110391D0 (en) | 1991-05-14 | 1991-07-03 | Agricultural Genetics Co | Biological control of pests |
US5215747A (en) | 1992-02-07 | 1993-06-01 | Uniroyal Chemical Company, Inc. | Composition and method for protecting plants from phytopathogenic fungi |
CA2132456A1 (fr) | 1992-04-03 | 1993-10-14 | Bert M. Zuckerman | Biopesticide nematocide de type bacillus thuringiensis |
ES2362721T3 (es) | 1992-07-01 | 2011-07-12 | Cornell Research Foundation Inc. | Inductor de la respuesta hipersensible en plantas. |
DE4238311A1 (de) | 1992-11-13 | 1994-05-19 | Hoechst Ag | Synergistische Mittel zur Bekämpfung von Insekten und Akariden |
DE19526465A1 (de) | 1994-08-16 | 1996-02-22 | Hoechst Schering Agrevo Gmbh | Entomopathogene Pilze enthaltende Mittel zur Bekämpfung von Insekten |
DE4445732A1 (de) | 1994-12-21 | 1996-06-27 | Hoechst Schering Agrevo Gmbh | Neue synergistische Mittel zur Bekämpfung von Insekten und Akarina |
DE19521487A1 (de) | 1995-06-13 | 1996-12-19 | Bayer Ag | Mercapto-triazolyl-dioxacycloalkane |
US6103228A (en) | 1997-05-09 | 2000-08-15 | Agraquest, Inc. | Compositions and methods for controlling plant pests |
PL198772B1 (pl) | 1997-05-09 | 2008-07-31 | Agraquest | Biologicznie czysta kultura Bacillus subtilis, jej metabolit i supernatant z hodowli szczepu, kompozycje do ochrony roślin i owoców przed szkodnikami, sposób ochrony lub leczenia roślin i owoców, agrastatyny, sposób izolowania supernatantu o aktywności owadobójczej |
US20030224936A1 (en) | 1999-03-13 | 2003-12-04 | Gerhard Kretzschmar | Seed treatment composition |
WO2000066773A2 (fr) * | 1999-04-30 | 2000-11-09 | Syngenta Limited | Procedes |
US6871446B1 (en) | 2000-10-23 | 2005-03-29 | Thomas T. Yamashita | Microbial blend compositions and methods for their use |
US6872562B2 (en) | 2001-01-16 | 2005-03-29 | The Board Of Trustees Of The University Of Arkansas, N.A. | Herbicide resistant dinitrogen fixing bacteria and method of use |
AR035858A1 (es) | 2001-04-23 | 2004-07-21 | Bayer Corp | Derivados de cromano 2,6-sustituidos,composiciones farmaceuticas,uso de dichos derivados para la manufactura de medicamentos utiles como agonistas adrenorreceptores beta-3 |
US20030068303A1 (en) | 2001-05-11 | 2003-04-10 | Selvig Thomas A. | Biologic-chemical fungicide compositions and methods of use |
DK1426371T3 (da) | 2001-08-20 | 2009-01-26 | Nippon Soda Co | Tetrazoyloximderivater og agrokemikalier der indeholder samme som aktivstof |
ATE463478T1 (de) | 2001-09-27 | 2010-04-15 | Kyorin Seiyaku Kk | Diaryletherderivat, dessen additionssalz und immunosuppressivum |
US20030166476A1 (en) | 2002-01-31 | 2003-09-04 | Winemiller Mark D. | Lubricating oil compositions with improved friction properties |
US6846858B2 (en) | 2002-04-24 | 2005-01-25 | Brenton L. Lemay | Artificial soil composition and methods of its making and use |
CN100445465C (zh) | 2003-03-24 | 2008-12-24 | 永丰馀造纸股份有限公司 | 非木材纤维覆盖席的制作方法 |
CN1201657C (zh) | 2003-03-25 | 2005-05-18 | 浙江省化工研究院 | 甲氧基丙烯酸甲酯类化合物杀菌剂 |
CN1475560A (zh) | 2003-07-14 | 2004-02-18 | 刘佳鸣 | 复合生物菌剂 |
JP4528939B2 (ja) | 2003-11-19 | 2010-08-25 | 株式会社サカタのタネ | 土壌微生物を格納したバイオセンサーおよびその利用 |
BRPI0510964A (pt) | 2004-05-10 | 2007-11-20 | Syngenta Participations Ag | composição pesticida e método de controle de pestes |
ATE458722T1 (de) | 2004-06-18 | 2010-03-15 | Basf Se | 1-methyl-3-trifluormethyl-pyrazol-4-carbonsäure (ortho-phenyl)-anilide und ihre verwendung als fungizid |
US20080108686A1 (en) | 2004-06-18 | 2008-05-08 | Basf Aktiengesellschaft | N-(Ortho-Phenyl)-1-Methyl-3-Difluoromethylpyrazole-4-Carboxanilides And Their Use As Fungicides |
TWI366438B (en) | 2004-08-12 | 2012-06-21 | Ishihara Sangyo Kaisha | Fungicidal composition containing acid amide derivative |
GB0418048D0 (en) | 2004-08-12 | 2004-09-15 | Syngenta Participations Ag | Method for protecting useful plants or plant propagation material |
GB0422401D0 (en) | 2004-10-08 | 2004-11-10 | Syngenta Participations Ag | Fungicidal compositions |
WO2006087373A1 (fr) | 2005-02-17 | 2006-08-24 | F. Hoffmann-La Roche Ag | Utilisation du rapport nt-proanp/nt-probnp pour diagnostiquer des dysfonctionnements cardiaques |
CN101213191B (zh) | 2005-03-30 | 2011-08-24 | (株)大熊制药 | 抗真菌三唑衍生物 |
JP2008540353A (ja) | 2005-05-07 | 2008-11-20 | メリアル リミテッド | 殺虫剤用置換フェニルエーテル |
CN1907024A (zh) | 2005-08-03 | 2007-02-07 | 浙江化工科技集团有限公司 | 取代甲氧基丙烯酸甲酯类化合物杀菌剂 |
EP1763998B1 (fr) | 2005-09-16 | 2007-05-23 | Syngenta Participations AG | Compositions fongicides |
TWI372752B (en) | 2005-12-22 | 2012-09-21 | Nihon Nohyaku Co Ltd | Pyrazinecarboxamide derivatives and plant disease controlling agents containing the same |
PL2017268T3 (pl) | 2006-05-08 | 2013-06-28 | Kumiai Chemical Industry Co | Pochodna 1,2-benzoizotiazolu, oraz środek zwalczający choroby roślin rolniczych lub ogrodniczych |
WO2008013622A2 (fr) | 2006-07-27 | 2008-01-31 | E. I. Du Pont De Nemours And Company | Amides azocycliques fongicides |
KR20080062876A (ko) | 2006-12-29 | 2008-07-03 | 주식회사 대웅제약 | 신규한 항진균성 트리아졸 유도체 |
CN101225074A (zh) | 2007-01-18 | 2008-07-23 | 青岛科技大学 | 一类含芳醚三氮唑化合物的合成及杀菌活性 |
CN101028009A (zh) | 2007-04-03 | 2007-09-05 | 盐城苏滨生物农化有限公司 | 己唑醇与枯草芽孢杆菌复配农药 |
BRPI0816948B1 (pt) | 2007-09-20 | 2018-01-23 | Basf Se | Composição fungicida, seus usos, agente fungicida, método para controlar fungos nocivos fitopatogênicos, e semente resistente a fungos nocivos fitopatogênicos |
TWI428091B (zh) | 2007-10-23 | 2014-03-01 | Du Pont | 殺真菌劑混合物 |
CN104381270B (zh) | 2008-01-15 | 2017-04-12 | 拜尔农科股份公司 | 包含四唑肟衍生物和杀真菌或杀虫活性物质的农药组合物 |
HUE026195T2 (en) | 2008-01-22 | 2016-05-30 | Dow Agrosciences Llc | 4-Amino-5-fluoropyrimidine derivatives as fungicides |
JP2011520970A (ja) | 2008-05-19 | 2011-07-21 | オーエスアイ・フアーマスーテイカルズ・インコーポレーテツド | 置換されたイミダゾピラジン類およびイミダゾトリアジン類 |
KR101698610B1 (ko) * | 2008-05-30 | 2017-01-20 | 다우 아그로사이언시즈 엘엘씨 | Qoi-내성 진균 병원체의 방제 방법 |
BRPI0920122B1 (pt) | 2008-10-15 | 2017-12-19 | Bayer Intellectual Property Gmbh | Ditiin-tetracarboximides and their uses for combating phytopathogenic fungi |
DE102009009240A1 (de) | 2009-02-17 | 2010-08-19 | Floragard Vertriebs GmbH für Gartenbau | Aufwuchsmedium für Pflanzen und Verfahren zur Herstellung eines solchen Aufwuchsmediums |
WO2010109436A1 (fr) | 2009-03-25 | 2010-09-30 | Carepro Bioscience (P) Ltd | Formulation microbienne conçue pour une utilisation étendue en agriculture |
US8551919B2 (en) | 2009-04-13 | 2013-10-08 | University Of Delaware | Methods for promoting plant health |
TWI508962B (zh) | 2009-04-22 | 2015-11-21 | Du Pont | 氮雜環醯胺之固體形態 |
EA031063B1 (ru) | 2009-05-06 | 2018-11-30 | Байер Кропсайенс Лп | Способ повышения жизнеспособности и/или урожайности сельскохозяйственных растений при практически несуществующем давлении патогенов |
CN101906075B (zh) | 2009-06-05 | 2012-11-07 | 中国中化股份有限公司 | 含取代苯胺基嘧啶基团的e-型苯基丙烯酸酯类化合物及其应用 |
BRPI1008143A2 (pt) | 2009-06-05 | 2015-08-25 | Basf Se | Mistura composição agroquimica metodo para o combatre de fungos novicios fitopatogenicos e material de propagação de planta |
CA2762512A1 (fr) | 2009-06-18 | 2010-12-23 | Basf Se | Composes de triazole portant un substituant soufre |
CN101697737B (zh) | 2009-11-09 | 2012-04-25 | 江苏省农业科学院 | 枯草芽孢杆菌三环唑复配可湿性杀菌粉剂及其应用 |
CN101697736B (zh) | 2009-11-09 | 2012-04-25 | 江苏省农业科学院 | 枯草芽孢杆菌丙环唑复配可湿性杀菌粉剂及其应用 |
ES2691726T3 (es) | 2010-01-04 | 2018-11-28 | Nippon Soda Co., Ltd. | Compuesto heterocíclico que contiene nitrógeno y germicida agrícola/hortícola |
WO2011099804A2 (fr) | 2010-02-12 | 2011-08-18 | Daewoong Pharmaceutical Co., Ltd. | Nouveaux dérivés de triazole antifongiques |
CN103037684A (zh) | 2010-03-01 | 2013-04-10 | 德拉华州大学 | 用于在植物中增加生物量、铁浓度以及对病原体的耐受性的组合物和方法 |
EA022448B1 (ru) | 2010-03-18 | 2016-01-29 | Басф Се | Фунгицидные композиции, содержащие фосфорастворимый микроорганизм и фунгицидно активное соединение |
MX2012010261A (es) | 2010-03-24 | 2012-10-03 | Syngenta Participations Ag | Mezclas pesticidas. |
WO2011147953A1 (fr) | 2010-05-28 | 2011-12-01 | Basf Se | Mélanges pesticides |
EP2579723A2 (fr) | 2010-06-09 | 2013-04-17 | Syngenta Participations AG | Mélanges des pesticides comprenant dérivés d'isoxazoline |
GB2481118A (en) | 2010-06-09 | 2011-12-14 | Syngenta Participations Ag | Pesticidal mixtures comprising enantiomerically enriched isoxazoline derivatives |
JP2012025735A (ja) | 2010-06-24 | 2012-02-09 | Sumitomo Chemical Co Ltd | 植物病害防除組成物及び植物病害防除方法 |
JP5857511B2 (ja) | 2010-08-10 | 2016-02-10 | 住友化学株式会社 | 植物病害防除組成物およびその用途 |
WO2012023143A1 (fr) | 2010-08-19 | 2012-02-23 | E. I. Du Pont De Nemours And Company | Pyrazoles fongicides |
WO2012037782A1 (fr) | 2010-09-20 | 2012-03-29 | Glaxo Group Limited | Composés tricycliques, leurs procédés de préparation et leurs utilisations |
US8623390B2 (en) | 2010-09-24 | 2014-01-07 | The United States Of America, As Represented By The Secretary Of Agriculture | Use of novel strains for biological control of pink rot infections in potato tubers |
CN103384471A (zh) | 2010-09-28 | 2013-11-06 | 贝克-安德伍德公司 | 方法以及含茉莉酸或相关化合物的组合物 |
JP2013542987A (ja) | 2010-11-16 | 2013-11-28 | ユニバーシティー オブ デラウェア | イネの成長を改善し、ヒ素の取り込みを制限するための組成物および方法 |
EP2460407A1 (fr) | 2010-12-01 | 2012-06-06 | Bayer CropScience AG | Combinaisons de substance actives comprenant du pyridyléthylbenzamide et d'autres substances actives |
WO2012076563A1 (fr) | 2010-12-08 | 2012-06-14 | Basf Se | Mélanges pesticides |
WO2012079073A1 (fr) | 2010-12-10 | 2012-06-14 | Auburn University | Agents d'inoculation incluant des bactéries bacillus pour l'induction de la production de composés organiques volatils chez les végétaux |
WO2012080415A1 (fr) | 2010-12-15 | 2012-06-21 | Syngenta Participations Ag | Mélanges pesticides |
ES2636678T3 (es) | 2011-05-31 | 2017-10-06 | Syngenta Participations Ag | Mezclas pesticidas que comprenden derivados isoxazolínicos |
US9241493B2 (en) | 2011-06-14 | 2016-01-26 | Bayer Intellectual Property Gmbh | Use of an enaminocarbonyl compound in combination with a biological control agent |
PE20140826A1 (es) | 2011-07-13 | 2014-07-09 | Basf Se | Compuestos sustituidos fungicidas de 2-[2-halogenalquil-4-(fenoxi)-fenil]-1-[1,2,4]triazol-1-il-etanol |
JP2014520833A (ja) | 2011-07-15 | 2014-08-25 | ビーエーエスエフ ソシエタス・ヨーロピア | 殺菌性フェニルアルキル−置換2−[2−クロロ−4−(4−クロロ−フェノキシ)−フェニル]−1−[1,2,4]トリアゾール−1−イル−エタノール化合物 |
EP2731934A1 (fr) | 2011-07-15 | 2014-05-21 | Basf Se | Composés de 2-[2-chloro-4-(dihalo-phénoxy)-phényl]-1-[1,2,4]triazol-1-yl-éthanol substitués par alkyle et aryle fongicides |
CA2840284A1 (fr) | 2011-07-15 | 2013-01-24 | Basf Se | Composes fongicides de 2-[2-chloro-4-(4-chloro-phenoxy)-phenyl]-1-[1,2,4]triazol-1-yl-ethanol substitue par alkyle |
BR112014002922A2 (pt) | 2011-08-15 | 2017-02-21 | Basf Se | compostos da fórmula i, processo de preparação de compostos da fórmula i, compostos da formula xii, viii e xi, composições agroquímicas, uso e semente |
WO2013024082A1 (fr) | 2011-08-15 | 2013-02-21 | Basf Se | Composés de 1-{2-cyclyloxy-2-[2-halogéno-4-(4-halogéno-phénoxy)-phényl]-éthyl}-1h-[1,2,4]triazole substitués fongicides |
KR20140054235A (ko) | 2011-08-15 | 2014-05-08 | 바스프 에스이 | 살진균 치환된 1-{2-[2-할로-4-(4-할로겐-페녹시)-페닐]-2-알콕시-2-시클릴-에틸}-1h-[1,2,4]트리아졸 화합물 |
CN103717578B (zh) | 2011-08-15 | 2016-12-21 | 巴斯夫欧洲公司 | 杀真菌的取代的1‑{2‑[2‑卤代‑4‑(4‑卤代苯氧基)苯基]‑2‑乙氧基乙基}‑1h‑[1,2,4]三唑化合物 |
KR20140080482A (ko) | 2011-08-15 | 2014-06-30 | 바스프 에스이 | 살진균 치환된 1-{2-[2-할로-4-(4-할로겐-페녹시)-페닐]-2-알콕시-3-메틸-부틸}-1h-[1,2,4]트리아졸 화합물 |
CN103732581B (zh) | 2011-08-15 | 2016-05-18 | 巴斯夫欧洲公司 | 杀真菌的取代的1-{2-[2-卤代-4-(4-卤代苯氧基)苯基]-2-炔氧基乙基}-1h-[1,2,4]三唑化合物 |
WO2013050302A1 (fr) | 2011-10-03 | 2013-04-11 | Syngenta Participations Ag | Dérivés d'isoxazoline utilisés comme composés insecticides |
RU2478290C2 (ru) | 2011-11-11 | 2013-04-10 | Общество с ограниченной ответственностью "Бациз" | Биопрепарат для стимуляции роста и защиты растений от болезней, повышения урожайности и почвенного плодородия |
CN104010502B (zh) | 2011-12-21 | 2016-08-24 | 巴斯夫欧洲公司 | 嗜球果伞素类型化合物在防治耐受Qo抑制剂的植物病原性真菌中的用途 |
TWI568721B (zh) | 2012-02-01 | 2017-02-01 | 杜邦股份有限公司 | 殺真菌之吡唑混合物 |
EP2649879A1 (fr) | 2012-04-10 | 2013-10-16 | Basf Se | Mélanges de pesticides contenant de fluxapyroxad |
KR20150013586A (ko) | 2012-04-27 | 2015-02-05 | 다우 아그로사이언시즈 엘엘씨 | 살충 조성물 및 그와 관련된 방법 |
JP6075182B2 (ja) | 2012-04-27 | 2017-02-08 | 住友化学株式会社 | テトラゾリノン化合物及びその用途 |
JP6107377B2 (ja) * | 2012-04-27 | 2017-04-05 | 住友化学株式会社 | テトラゾリノン化合物及びその用途 |
US9483544B2 (en) | 2012-05-25 | 2016-11-01 | Crimson Hexagon, Inc. | Systems and methods for calculating category proportions |
US20150183493A1 (en) | 2012-07-04 | 2015-07-02 | Paul Francis Zwaan | Shock mitigation apparatus |
GB2504141B (en) | 2012-07-20 | 2020-01-29 | Flexenable Ltd | Method of reducing artefacts in an electro-optic display by using a null frame |
WO2014029697A1 (fr) | 2012-08-22 | 2014-02-27 | Basf Se | Mélanges ternaires fongicides comprenant du fluaziname |
JP6142753B2 (ja) | 2012-09-28 | 2017-06-07 | 住友化学株式会社 | テトラゾリノン化合物及びその用途 |
JP6142752B2 (ja) | 2012-09-28 | 2017-06-07 | 住友化学株式会社 | テトラゾリノン化合物及びその用途 |
MX2015003719A (es) | 2012-10-01 | 2015-06-24 | Basf Se | Mezclas plaguicidas. |
WO2014053405A1 (fr) | 2012-10-01 | 2014-04-10 | Basf Se | Mélange à activité pesticide comprenant des composés anthranilamides |
WO2014060177A1 (fr) | 2012-10-16 | 2014-04-24 | Syngenta Participations Ag | Compositions fongicides |
US20160289130A1 (en) | 2012-11-15 | 2016-10-06 | Basf Corporation | Mulch and Potting Soil Compositions Containing Microorganisms and Related Methods |
WO2014079772A1 (fr) | 2012-11-22 | 2014-05-30 | Basf Se | Mélanges pesticides |
WO2014079841A1 (fr) | 2012-11-22 | 2014-05-30 | Basf Se | Mélanges pesticides |
WO2014079771A1 (fr) | 2012-11-22 | 2014-05-30 | Basf Se | Mélanges pesticides |
WO2014079804A1 (fr) | 2012-11-22 | 2014-05-30 | Basf Se | Mélanges pesticides |
WO2014079728A1 (fr) | 2012-11-22 | 2014-05-30 | Basf Se | Mélanges pesticides |
AU2013349890B2 (en) | 2012-11-22 | 2017-04-13 | Basf Corporation | Pesticidal mixtures |
WO2014079724A1 (fr) | 2012-11-22 | 2014-05-30 | Basf Se | Mélanges pesticides |
WO2014079770A1 (fr) | 2012-11-22 | 2014-05-30 | Basf Se | Mélanges pesticides |
WO2014079774A1 (fr) | 2012-11-22 | 2014-05-30 | Basf Se | Mélanges pesticides |
EP2922403A1 (fr) | 2012-11-22 | 2015-09-30 | BASF Corporation | Mélanges pesticides |
PL2922399T3 (pl) | 2012-11-22 | 2020-11-02 | Basf Corporation | Mieszaniny szkodnikobójcze |
WO2014079766A1 (fr) | 2012-11-22 | 2014-05-30 | Basf Se | Mélanges pesticides |
WO2014079764A1 (fr) | 2012-11-22 | 2014-05-30 | Basf Se | Mélanges pesticides |
WO2014079730A1 (fr) | 2012-11-23 | 2014-05-30 | Basf Se | Mélanges pesticides |
WO2014079752A1 (fr) | 2012-11-23 | 2014-05-30 | Basf Se | Mélanges pesticides |
WO2014079754A1 (fr) | 2012-11-23 | 2014-05-30 | Basf Se | Mélanges pesticides |
WO2014079813A1 (fr) | 2012-11-23 | 2014-05-30 | Basf Se | Mélanges pesticides |
WO2014079769A1 (fr) | 2012-11-23 | 2014-05-30 | Basf Se | Mélanges pesticides |
EP2927218B1 (fr) | 2012-11-29 | 2018-07-04 | Sumitomo Chemical Company, Limited | Composé de tétrazolinone et son utilisation |
WO2014086851A1 (fr) | 2012-12-04 | 2014-06-12 | Basf Agro B.V., Arnhem (Nl) | Compositions comprenant un extrait de quillay et un inhibiteur fongicide de complexe respiratoire iii au niveau du site qo |
WO2014086854A1 (fr) | 2012-12-04 | 2014-06-12 | Basf Agro B.V., Arnhem (Nl) | Compositions comprenant un extrait de quillay et un régulateur de croissance de plante |
WO2014086853A1 (fr) | 2012-12-04 | 2014-06-12 | Basf Agro B.V., Arnhem (Nl) | Compositions comprenant un extrait de quillay et un composé fongicide |
WO2014086848A1 (fr) | 2012-12-04 | 2014-06-12 | Basf Agro B.V., Arnhem (Nl) | Compositions comprenant un extrait de quillay et un principe actif insecticide |
WO2014086850A1 (fr) | 2012-12-04 | 2014-06-12 | Basf Agro B.V., Arnhem (Nl) | Compositions comprenant un extrait de quillay et un inhibiteur fongicide du complexe respiratoire ii |
WO2014086856A1 (fr) | 2012-12-04 | 2014-06-12 | Basf Agro B.V., Arnhem (Nl) | Compositions comprenant un extrait de quillay et un biopesticide |
US10759767B2 (en) | 2012-12-20 | 2020-09-01 | BASF Agro B.V. | Compositions comprising a triazole compound |
US20150313225A1 (en) | 2012-12-20 | 2015-11-05 | Basf Se | Compositions Comprising a Triazole Compound |
BR112015018853B1 (pt) | 2013-03-20 | 2021-07-13 | Basf Corporation | Mistura, composição agroquímica, método para controlar fungos fitopatogênicos, método para proteção do material de propagação dos vegetais e semente revestida |
CN105142405B (zh) | 2013-03-20 | 2018-04-20 | 巴斯夫公司 | 包含枯草芽孢杆菌菌株和农药的协同增效组合物 |
BR112015029576B1 (pt) | 2013-05-28 | 2020-09-15 | Syngenta Participations Ag | Uso de derivados do ácido tetrâmico como nematicidas e método para redução de danos causados por nematódeos a uma planta |
JP6337896B2 (ja) * | 2013-05-29 | 2018-06-06 | 住友化学株式会社 | テトラゾリノン化合物及びその用途 |
EP3010344B1 (fr) | 2013-06-18 | 2017-11-15 | Basf Se | Mélanges fongicides i comprenant des fongicides de type strobilurine |
EP2815649A1 (fr) | 2013-06-18 | 2014-12-24 | Basf Se | Mélanges fongicides II comprenant des fongicides de type strobilurine |
US10512267B2 (en) | 2013-07-08 | 2019-12-24 | BASF Agro, B.V. | Compositions comprising a triazole compound and a biopesticide |
CN105555138A (zh) | 2013-07-22 | 2016-05-04 | 住友化学株式会社 | 植物病害防治组合物及其用途 |
ES2731349T3 (es) | 2013-07-22 | 2019-11-15 | Sumitomo Chemical Co | Composición para el control de enfermedades de las plantas y su uso |
ES2664802T3 (es) | 2013-07-22 | 2018-04-23 | Sumitomo Chemical Company Limited | Composición para el control de enfermedades de las plantas y su uso |
EP2835052A1 (fr) | 2013-08-07 | 2015-02-11 | Basf Se | Mélanges fongicides comprenant des pyrimidines fongicides |
TWI652014B (zh) | 2013-09-13 | 2019-03-01 | 美商艾佛艾姆希公司 | 雜環取代之雙環唑殺蟲劑 |
WO2015051171A1 (fr) * | 2013-10-02 | 2015-04-09 | Bio-Rad Laboratories, Inc. | Innovation pour mélange de dosage |
WO2015056806A1 (fr) * | 2013-10-17 | 2015-04-23 | 住友化学株式会社 | Composé tétrazolinone et application associée |
CN105683169B (zh) * | 2013-10-28 | 2018-11-06 | 住友化学株式会社 | 四唑啉酮化合物及其用途 |
CN105939602B (zh) | 2014-01-30 | 2020-01-14 | 巴斯夫欧洲公司 | 作为在作物保护中的辅助剂的不对称甲缩醛和缩醛 |
EP2865265A1 (fr) | 2014-02-13 | 2015-04-29 | Bayer CropScience AG | Combinaisons de composés actifs comprenant des composés phénylamidine et agents de lutte biologique |
US10238106B2 (en) | 2014-03-12 | 2019-03-26 | Basf Se | Carbonates of alcohol alkoxylates as adjuvants for crop protection |
EP3119200A4 (fr) | 2014-03-20 | 2017-08-23 | Mitsui Chemicals Agro, Inc. | Composition de lutte contre une maladie de plante, et procédé de lutte contre une maladie de plante par application de cette dernière |
WO2015147313A1 (fr) * | 2014-03-28 | 2015-10-01 | 住友化学株式会社 | Composé tétrazolinone et application associée |
US10694742B2 (en) | 2014-05-06 | 2020-06-30 | Basf Se | Composition comprising a pesticide and a hydroxyalkyl polyoxylene glycol ether |
WO2015177021A1 (fr) | 2014-05-23 | 2015-11-26 | Basf Se | Mélanges comprenant une souche de bacillus et un pesticide |
EP2962568A1 (fr) * | 2014-07-01 | 2016-01-06 | Basf Se | Mélanges comprenant une souche de Bacillus amyloliquefaciens ssp. plantarum et pesticide |
WO2015180985A1 (fr) | 2014-05-27 | 2015-12-03 | Basf Se | Mélanges ternaires comprenant des biopesticides, des fongicides contre les phycomycètes et des fongicides à base de sdhi |
WO2015181009A1 (fr) | 2014-05-27 | 2015-12-03 | Basf Se | Mélanges ternaires comprenant des biopesticides et des fongicides qoi et des fongicides sdhi |
WO2015180999A1 (fr) | 2014-05-27 | 2015-12-03 | Basf Se | Mélanges ternaires comprenant des biopesticides et des fongicides sdhi et des fongicides du type azoles |
WO2015180983A1 (fr) | 2014-05-27 | 2015-12-03 | Basf Se | Mélanges comprenant des bactéries de fixation de l'azote, des biopesticides et des pesticides chimiques |
WO2015181008A1 (fr) | 2014-05-27 | 2015-12-03 | Basf Se | Mélanges ternaires comprenant des biopesticides et des fongicides chimiques et des insecticides chimiques |
WO2015180987A1 (fr) | 2014-05-27 | 2015-12-03 | Basf Se | Mélanges ternaires comprenant des biopesticides et des fongicides contre les phycomycètes et des fongicides à base de qol ou phénylpyrrole |
WO2015181035A1 (fr) * | 2014-05-30 | 2015-12-03 | Basf Se | Mélanges fongicides à base de dérivés de 1,4-dithiine |
KR102343802B1 (ko) | 2014-06-09 | 2021-12-28 | 수미토모 케미칼 컴퍼니 리미티드 | 피리딘 화합물의 제조 방법 |
CN106793776A (zh) | 2014-06-25 | 2017-05-31 | 巴斯夫农业公司 | 农药组合物 |
KR102469841B1 (ko) | 2014-07-14 | 2022-11-22 | 바스프 에스이 | 살충 조성물 |
WO2016071164A1 (fr) | 2014-11-07 | 2016-05-12 | Basf Se | Mélanges pesticides |
UA120628C2 (uk) | 2014-11-07 | 2020-01-10 | Басф Се | Пестицидні суміші |
WO2016071168A1 (fr) | 2014-11-07 | 2016-05-12 | Basf Se | Mélanges pesticides |
WO2016071246A1 (fr) | 2014-11-07 | 2016-05-12 | Basf Se | Mélanges pesticides |
WO2016078995A1 (fr) | 2014-11-21 | 2016-05-26 | BASF Agro B.V. | Compositions pesticides |
WO2016091675A1 (fr) | 2014-12-12 | 2016-06-16 | Basf Se | Procédé d'amélioration de la santé de plante |
WO2016174042A1 (fr) | 2015-04-27 | 2016-11-03 | BASF Agro B.V. | Compositions pesticides |
EP2910126A1 (fr) | 2015-05-05 | 2015-08-26 | Bayer CropScience AG | Combinaisons de composés actifs à propriétés insecticides |
BR112018015526A2 (pt) | 2016-02-26 | 2018-12-26 | Basf Se | misturas fungicidas, composição fungicida, métodos para controlar fungos fitopatogênicos, para melhorar a saúde de plantas e para a proteção de material de propagação vegetal e material de propagação de plantas |
WO2017153200A1 (fr) | 2016-03-10 | 2017-09-14 | Basf Se | Mélanges fongicides iii contenant des fongicides de type strobilurine |
US11241012B2 (en) | 2016-03-16 | 2022-02-08 | Basf Se | Use of tetrazolinones for combating resistant phytopathogenic fungi on soybean |
RU2746463C2 (ru) | 2016-03-16 | 2021-04-14 | Басф Се | Применение тетразолинонов для борьбы с устойчивыми фитопатогенными грибами на зерновых путем обработки семян |
WO2017157923A1 (fr) | 2016-03-16 | 2017-09-21 | Basf Se | Utilisation de tétrazolinones pour lutter contre des champignons phytopathogènes résistants sur des plantes agricoles |
EP3429358A1 (fr) | 2016-03-16 | 2019-01-23 | Basf Se | Utilisation de tétrazolinones pour lutter contre des champignons phytopathogènes résistants sur des fruits |
KR102445887B1 (ko) | 2016-04-21 | 2022-09-21 | 아스트로사이트 파마슈티컬스, 인코포레이티드 | 신경계 및 심혈관계 병태 치료를 위한 화합물 및 방법 |
-
2017
- 2017-03-14 RU RU2018135845A patent/RU2754614C2/ru active
- 2017-03-14 UA UAA201810052A patent/UA125210C2/uk unknown
- 2017-03-14 CA CA3015744A patent/CA3015744C/fr active Active
- 2017-03-14 JP JP2018548725A patent/JP6903074B2/ja active Active
- 2017-03-14 US US16/083,898 patent/US10905122B2/en active Active
- 2017-03-14 EP EP17709719.3A patent/EP3429357A1/fr active Pending
- 2017-03-14 WO PCT/EP2017/055946 patent/WO2017157910A1/fr active Application Filing
Also Published As
Publication number | Publication date |
---|---|
RU2754614C2 (ru) | 2021-09-03 |
EP3429357A1 (fr) | 2019-01-23 |
JP2019508466A (ja) | 2019-03-28 |
CA3015744A1 (fr) | 2017-09-21 |
RU2018135845A3 (fr) | 2020-05-28 |
WO2017157910A1 (fr) | 2017-09-21 |
RU2018135845A (ru) | 2020-04-16 |
US20190082695A1 (en) | 2019-03-21 |
US10905122B2 (en) | 2021-02-02 |
JP6903074B2 (ja) | 2021-07-14 |
UA125210C2 (uk) | 2022-02-02 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CA3015744C (fr) | Utilisation de 1-[2-[[1-(4-chlorophenyle)pyrazol-3-yl]oxymethyle]-3-methyle-phenyle]-4-methyle-tetrazol-5-one pour lutter contre les champignonsphytopathogenes resistants sur les cereales | |
US11241012B2 (en) | Use of tetrazolinones for combating resistant phytopathogenic fungi on soybean | |
WO2017157923A1 (fr) | Utilisation de tétrazolinones pour lutter contre des champignons phytopathogènes résistants sur des plantes agricoles | |
US11425909B2 (en) | Use of tetrazolinones for combating resistant phytopathogenic fungi on fruits | |
TWI651048B (zh) | 藉由使用殺真菌組成物增加產量之方法 | |
EP2531025B1 (fr) | Méthode de traitement des infections fongiques, compositions fongicides et leur utilisation | |
RU2746463C2 (ru) | Применение тетразолинонов для борьбы с устойчивыми фитопатогенными грибами на зерновых путем обработки семян | |
EA012612B1 (ru) | Способ борьбы с грибковыми заболеваниями бобовых культур | |
KR20090108735A (ko) | 치환된 1-메틸피라졸-4-일카르복스아닐리드를 포함하는 살진균 혼합물 | |
JP5502854B2 (ja) | 菌類感染から大豆を保護する方法 | |
WO2017110864A1 (fr) | Composition de lutte contre des maladies végétales et son application | |
WO2019043183A1 (fr) | Procédé de lutte contre les nuisibles du riz dans le riz | |
EP3915379A1 (fr) | Mélanges de pesticides | |
PL180374B1 (pl) | kompozycja do ochrony roslin przed zakazeniami grzybiczymi i owadamioraz sposób ochrony roslin przed zakazeniami grzybiczymi i owadami PL PL PL PL PL PL PL | |
WO2007071656A1 (fr) | Procede pour lutter contre les attaques de rouille chez les legumineuses | |
EP2807924A1 (fr) | Procédé pour lutter contre des pathogènes fongiques de gazon | |
CN112584704A (zh) | 杀真菌活性化合物i衍生物及其混合物在种子施用和处理方法中的用途 | |
JP3562035B2 (ja) | アズキ類の増収方法 | |
RU2746810C2 (ru) | Эмульгирующийся концентрат, содержащий триазольный фунгицид, амид жирной кислоты и ароматический углеводород | |
EP0092961B1 (fr) | Composition fongicide | |
WO2022090071A1 (fr) | Utilisation de méfenpyrdiéthyl pour lutter contre des champignons phytopathogènes | |
US20230397603A1 (en) | Fertilizer compatible agrochemical suspensions | |
EP3047731A1 (fr) | Procédé de lutte contre la rouille du soja comprenant le traitement du soja avec des (2E)-2-[3-substitués-2 [[(E)-[(2E)-2-alkoxyimino-1-méthyl-2-phényl-ethylidene]amino]oxyméthyl]phényl]-2-méthoxy-imino-N-méthyl-acétamides | |
EP3031325A1 (fr) | Procédé de lutte contre la rouille du soja comprenant le traitement du soja avec des (2E)-2-[2-[[1-(2,4-substitués-phényl)pyrazol-3-yl]oxyméthyl]-3-substitués phényl]-2-méthoxyimino-n-méthyl-acétamides | |
EP3029025A1 (fr) | Procédé de lutte contre la rouille du soja comprenant le traitement du soja avec des (2E)-2-méthoxyimino-2 [2 [[(E)-[(2E)-2-alkoxyimino-1-méthyl-alk-3-enylidène]amino]oxyméthyl]-phényl]-n-méthyl-acétamides |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
EEER | Examination request |
Effective date: 20220309 |
|
EEER | Examination request |
Effective date: 20220309 |
|
EEER | Examination request |
Effective date: 20220309 |
|
EEER | Examination request |
Effective date: 20220309 |
|
EEER | Examination request |
Effective date: 20220309 |
|
EEER | Examination request |
Effective date: 20220309 |
|
EEER | Examination request |
Effective date: 20220309 |
|
EEER | Examination request |
Effective date: 20220309 |
|
EEER | Examination request |
Effective date: 20220309 |